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Use of CytoSorb® as a therapeutic option in a critically ill patient with acute respiratory distress syndrome caused by influenza A (H1N1) pneumonia: A case report

Acute respiratory distress syndrome is an acute inflammatory lung process, which leads to protein-rich nonhydrostatic pulmonary edema, refractory hypoxemia, and lung “stiffness”. There are a number of therapies that are currently being investigated in the treatment of sepsis; one of the most promisi...

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Autores principales: Kovacevic, Pedja, Tomic, Boris, Kovacevic, Tijana, Dragic, Sasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033202/
https://www.ncbi.nlm.nih.gov/pubmed/33850832
http://dx.doi.org/10.4103/IJCIIS.IJCIIS_56_20
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author Kovacevic, Pedja
Tomic, Boris
Kovacevic, Tijana
Dragic, Sasa
author_facet Kovacevic, Pedja
Tomic, Boris
Kovacevic, Tijana
Dragic, Sasa
author_sort Kovacevic, Pedja
collection PubMed
description Acute respiratory distress syndrome is an acute inflammatory lung process, which leads to protein-rich nonhydrostatic pulmonary edema, refractory hypoxemia, and lung “stiffness”. There are a number of therapies that are currently being investigated in the treatment of sepsis; one of the most promising treatment options at this moment is cytokine removal by hemoperfusion (CytoSorb(®)). We present the case of a 29-year-old male patient who was admitted to the Medical Intensive Care Unit in a state of multiple organ dysfunction and massive bilateral pneumonia caused by influenza type A. The patient was healthy before hospital admission. Due to acute respiratory failure and altered state of consciousness, the patient was intubated using analgosedation and connected to a controlled mechanical ventilation mode immediately after admission. The initial computed tomography scan showed massive bilateral pneumonia, and few days later, the patient's condition progressively worsened and he developed signs of multiorgan failure. Given the patient's progressing hemodynamic instability and uncontrolled inflammatory response, a CytoSorb(®) adsorber was added into the continuous renal replacement therapy circuit. The combination of pharmacotherapy, supportive measures, and application of CytoSorb(®) resulted with complete recovery of the patient (hemodynamic stability improved as evidenced by decreased vasopressor requirements).
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spelling pubmed-80332022021-04-12 Use of CytoSorb® as a therapeutic option in a critically ill patient with acute respiratory distress syndrome caused by influenza A (H1N1) pneumonia: A case report Kovacevic, Pedja Tomic, Boris Kovacevic, Tijana Dragic, Sasa Int J Crit Illn Inj Sci Case Report Acute respiratory distress syndrome is an acute inflammatory lung process, which leads to protein-rich nonhydrostatic pulmonary edema, refractory hypoxemia, and lung “stiffness”. There are a number of therapies that are currently being investigated in the treatment of sepsis; one of the most promising treatment options at this moment is cytokine removal by hemoperfusion (CytoSorb(®)). We present the case of a 29-year-old male patient who was admitted to the Medical Intensive Care Unit in a state of multiple organ dysfunction and massive bilateral pneumonia caused by influenza type A. The patient was healthy before hospital admission. Due to acute respiratory failure and altered state of consciousness, the patient was intubated using analgosedation and connected to a controlled mechanical ventilation mode immediately after admission. The initial computed tomography scan showed massive bilateral pneumonia, and few days later, the patient's condition progressively worsened and he developed signs of multiorgan failure. Given the patient's progressing hemodynamic instability and uncontrolled inflammatory response, a CytoSorb(®) adsorber was added into the continuous renal replacement therapy circuit. The combination of pharmacotherapy, supportive measures, and application of CytoSorb(®) resulted with complete recovery of the patient (hemodynamic stability improved as evidenced by decreased vasopressor requirements). Wolters Kluwer - Medknow 2020 2020-12-29 /pmc/articles/PMC8033202/ /pubmed/33850832 http://dx.doi.org/10.4103/IJCIIS.IJCIIS_56_20 Text en Copyright: © 2020 International Journal of Critical Illness and Injury Science https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Kovacevic, Pedja
Tomic, Boris
Kovacevic, Tijana
Dragic, Sasa
Use of CytoSorb® as a therapeutic option in a critically ill patient with acute respiratory distress syndrome caused by influenza A (H1N1) pneumonia: A case report
title Use of CytoSorb® as a therapeutic option in a critically ill patient with acute respiratory distress syndrome caused by influenza A (H1N1) pneumonia: A case report
title_full Use of CytoSorb® as a therapeutic option in a critically ill patient with acute respiratory distress syndrome caused by influenza A (H1N1) pneumonia: A case report
title_fullStr Use of CytoSorb® as a therapeutic option in a critically ill patient with acute respiratory distress syndrome caused by influenza A (H1N1) pneumonia: A case report
title_full_unstemmed Use of CytoSorb® as a therapeutic option in a critically ill patient with acute respiratory distress syndrome caused by influenza A (H1N1) pneumonia: A case report
title_short Use of CytoSorb® as a therapeutic option in a critically ill patient with acute respiratory distress syndrome caused by influenza A (H1N1) pneumonia: A case report
title_sort use of cytosorb® as a therapeutic option in a critically ill patient with acute respiratory distress syndrome caused by influenza a (h1n1) pneumonia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033202/
https://www.ncbi.nlm.nih.gov/pubmed/33850832
http://dx.doi.org/10.4103/IJCIIS.IJCIIS_56_20
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